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 Newly diagnosed families should contact us. Welcome to the Children's Gaucher ("go-shay") Research Fund. We are a non-profit organization, that raises funds to coordinate and support research to find a cure for Type 2 and Type 3 Gauchers Disease. |
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How the fund began
Gregory's Legacy
San Jose Mercury News
24 February 1998
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A site for Families and Physicians
Newly diagnosed families should contact us. If you are a Gauchers disease Type 2 or Type 3 family, or a physician concerned about Gauchers disease, the Children's Gauchers Disease Research Fund web site can help. Follow the links to locate current research findings, share information with others battling this disease, and connect to valuable resources throughout the world. We also encourage you to find out more about the people affected by Gauchers disease in our Helping Hands Newsletter and by visiting Family Stories. You can contact us directly: research@childrensgaucher.org.
A site for Contributors
If you are an individual, corporation, or organization interested in donating time or money to help find a cure for Type 2 and Type 3 Gauchers Disease, we invite you to learn about the fund and its founders. We also encourage you to read about some of the children and families affected by Gauchers disease.
What makes us different is that 100% of every donation to the Children's Gauchers Disease Research Fund goes to medical research. There are no salaries. There are no administrative costs. All costs for postage, printing, web site development, etc. are either donated, or paid for by the founders. Why? Your generosity is not taken lightly. Together we will find a cure for Gauchers Disease. Together we will find a cure for these children. |
